A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3767054



Internal ID18962575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:120494678..120497454hg38UCSC Ensembl
chr9:123256956..123259732hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg382777
hg192777
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1077179
Supporting Variants
SamplesKWP1
Known GenesCDK5RAP2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3767054
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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